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Safety of bendamustine for the treatment of indolent non-Hodgkin lymphoma: a UK real-world experience.
Shotton, Rohan; Broadbent, Rachel; Alchawaf, Alia; Mohamed, Mohamed Bakri; Gibb, Adam; Martinez-Calle, Nicolás; Fox, Christopher P; Bishton, Mark; Pender, Alexandra; Gleeson, Mary; Cunningham, David; Davies, Andrew; Yadollahi, Sina; Eyre, Toby A; Collins, Graham; Djebbari, Faouzi; Kassam, Shireen; Garland, Paula; Watts, Emily; Osborne, Wendy; Townsend, William; Pocock, Rachael; Ahearne, Matthew J; Miall, Fiona; Wang, Xin; Linton, Kim M.
Afiliación
  • Shotton R; The Christie NHS Foundation Trust, Manchester, United Kingdom.
  • Broadbent R; The Christie NHS Foundation Trust, Manchester, United Kingdom.
  • Alchawaf A; The Christie NHS Foundation Trust, Manchester, United Kingdom.
  • Mohamed MB; The Christie NHS Foundation Trust, Manchester, United Kingdom.
  • Gibb A; The Christie NHS Foundation Trust, Manchester, United Kingdom.
  • Martinez-Calle N; Clinical Haematology, Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
  • Fox CP; Clinical Haematology, Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
  • Bishton M; School of Medicine, University of Nottingham, Nottingham, United Kingdom.
  • Pender A; Clinical Haematology, Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
  • Gleeson M; Department of Medicine, The Royal Marsden Hospital, London, United Kingdom.
  • Cunningham D; Haematology, The Royal Marsden Hospital, London, United Kingdom.
  • Davies A; Haematology, The Royal Marsden Hospital, London, United Kingdom.
  • Yadollahi S; Cancer Research UK/NIHE Experimental Cancer Medicines Centre, University of Southampton, Southampton, United Kingdom.
  • Eyre TA; Haematology, Haematology and Cancer Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
  • Collins G; Haematology, Haematology and Cancer Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
  • Djebbari F; Haematology, Haematology and Cancer Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
  • Kassam S; Haematology, Haematology and Cancer Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
  • Garland P; Haematology, King's College Hospital, London, United Kingdom.
  • Watts E; Haematology, King's College Hospital, Princess Royal Site, Kent, United Kingdom.
  • Osborne W; Haematology, Freeman Hospital, Newcastle, United Kingdom.
  • Townsend W; Haematology, Freeman Hospital, Newcastle, United Kingdom.
  • Pocock R; Haematology, University College Hospital London, London, United Kingdom.
  • Ahearne MJ; Haematology, University College Hospital London, London, United Kingdom.
  • Miall F; Haematology, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.
  • Wang X; Haematology, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.
  • Linton KM; Statistics Group, Clinical Outcome Unit, Digital Services, The Christie NHS Foundation Trust, Manchester, United Kingdom.
Blood Adv ; 8(4): 878-888, 2024 Feb 27.
Article en En | MEDLINE | ID: mdl-37967358
ABSTRACT
ABSTRACT Bendamustine is among the most effective chemotherapeutics for indolent B-cell non-Hodgkin lymphomas (iNHL), but trial reports of significant toxicity, including opportunistic infections and excess deaths, led to prescriber warnings. We conducted a multicenter observational study evaluating bendamustine toxicity in real-world practice. Patients receiving at least 1 dose of bendamustine with/without rituximab (R) for iNHL were included. Demographics, lymphoma and treatment details, and grade 3 to 5 adverse events (AEs) were analyzed and correlated. In total, 323 patients were enrolled from 9 National Health Service hospitals. Most patients (96%) received bendamustine-R, and 46%, R maintenance. Overall, 21.7% experienced serious AEs (SAE) related to treatment, including infections in 12%, with absolute risk highest during induction (63%), maintenance (20%), and follow-up (17%) and the relative risk highest during maintenance (54%), induction (34%), and follow-up (28%). Toxicity led to permanent treatment discontinuation for 13% of patients, and 2.8% died of bendamustine-related infections (n = 5), myelodysplastic syndrome (n = 3), and cardiac disease (n = 1). More SAEs per patient were reported in patients with mantle cell lymphoma, poor preinduction performance status (PS), poor premaintenance PS, and abnormal preinduction total globulins and in those receiving growth factors. Use of antimicrobial prophylaxis was variable, and 3 of 10 opportunistic infections occurred despite prophylaxis. In this real-world analysis, bendamustine-related deaths and treatment discontinuation were similar to those of trial populations of younger, fitter patients. Poor PS, mantle cell histology, and maintenance R were potential risk factors. Infections, including late onset events, were the most common treatment-related SAE and cause of death, warranting extended antimicrobial prophylaxis and infectious surveillance, especially for maintenance-treated patients.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Linfoma no Hodgkin / Infecciones Oportunistas / Linfoma de Células B / Linfoma de Células del Manto / Antiinfecciosos Límite: Adult / Humans País/Región como asunto: Europa Idioma: En Revista: Blood Adv Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Linfoma no Hodgkin / Infecciones Oportunistas / Linfoma de Células B / Linfoma de Células del Manto / Antiinfecciosos Límite: Adult / Humans País/Región como asunto: Europa Idioma: En Revista: Blood Adv Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido